Search results for "malformations"

Historia natural de 30 casos de cavernomas: un seguimiento de dos décadas en el Estado de Paraíba, Brasil

2019

Introducción: Los cavernomas son malformaciones vasculares de bajo flujo que ocurren principalmente en el cerebro y, menos frecuentemente, en la médula espinal. Son lesiones raras y representan alrededor del 5-13% de las malformaciones vasculares del sistema nervioso central. Objetivos: Evaluar el seguimiento de 30 casos de pacientes diagnosticados con cavernomas y describir los hallazgos clínicos, epidemiológicos, topográficos, evolutivos y la conducta terapéutica en un período de 22 años. Metodología: Se trata de un estudio observacional, transversal, de carácter cuantitativo, que incluye pacientes diagnosticados con cavernomas, a través de la recolección de datos en los Servicios de Neur…

Catheter venography for the assessment of internal jugular veins and azygous vein: position statement by expert panel of the International Society fo…

2013

This document by an expert panel of the International Society for Neurovascular Disease is aimed at presenting current technique and interpretation of catheter venography of the internal jugular veins, azygous vein and other veins draining the central nervous system. Although interventionalists agree on general rules, significant differences exist in terms of details of venographic technique and interpretations of angiographic pictures. It is also suggested that debatable findings should be investigated using multimodal diagnostics. Finally, the authors recommend that any publication on chronic cerebrospinal venous insufficiency should include detailed description of venographic technique u…

Prenatal diagnosis of cerebral malformation with an uncertain prognosis: a study concerning couple's information and consequences on pregnancy.

2004

Abstract Fetal ultrasound (FU) is used during almost all pregnancies and makes a large contribution to the identification of fetal malformation. It is particularly difficult to announce a malformation, particularly those affecting the brain, because there are often doubts concerning both the diagnosis and the prognosis. Aim. – The aim of this study was to analyze how imaging for prenatal screening is organized and how couples are managed and supported. We concentrated on the procedures used to inform couples: content, method of delivery and consequences. Method. –: Study amongst large multidisciplinary centers in Paris and the Paris region, by semi-directed interviews using a questionnaire.…

The Challenges of the European Anorectal Malformations-Net Registry

2015

Item does not contain fulltext Anorectal malformations (ARM) have a low prevalence, patients need specialized surgical care, and in many cases, patients born with ARM even need life-long aftercare. Due to its low prevalence most patients are still treated in low-volume pediatric surgical centers without any adequate monitoring of the outcome. Data on prevalence, comparison of different surgical techniques, and prospective outcome measurements are still scarce and difficult to interpret. In 2010, a consortium was founded (ARM-Net consortium) including several European pediatric surgical centers to collaborate more in research and share knowledge on ARM. One of the structures started by the c…

Hatching Success of Caretta caretta on a Mediterranean Volcanic Beach: Impacts from Environmental Parameters and Substrate Composition

2022

New data on the potential impact of environmental parameters and the mineralogical nature of the substrate on the hatching success of the loggerhead sea turtle Caretta caretta on a volcanic beach on Linosa Island in the central Mediterranean Sea are reported. During 2 years of investigation (2018-19), five nests were observed. The temperature and moisture of the nests were determined along with the grain size and mineralogical nature of the substrate. The temperature values of the nests recorded at depths of 5 and 35 cm showed an average temperature incubation of 32.2°C ± 1.4°C and 32.8°C ± 1.6°C, respectively, with peaks close to 37°C. The sedimentological analysis carried out on two cores…

Morphometric analysis of the shells of the Genus Bolivina from the Gulf of Gela (Sicilian Channel, Italy): a valid classification instrument?

2010

UNA RARA COMPLICANZA DEL DIVERTICOLO INTRALUMINALE DEL DUODENO

1986

The Authors report a case of intraluminal diverticulum of the duodenum complicated by endodiverticulum litiasis

Multiple Congenital Colonic Stenosis: Case Report and Review of the Literature

2015

Congenital malformations affecting the colon are rare pediatric conditions often presenting as obstruction. Colonic atresia accounts for 5-­‐10% of atresia in newborns, stenosis is even more rare.Since 1968, only 16 cases of CCS have been reported in literature (Table 1). Because of the rarity of the disease, little is known about this uncommon condition and management is still controversial. We present a case of multiple congenital colonic stenosis and review the literature with a special focus on management of CCS. To the authors' knowledge, multiple congenital colonic stenosis has not been reported previously in the literature.

ROLE OF ENDOVASCULAR EMBOLIZATION IN THE MULTIDISCIPLINARY MANAGEMENT OF RUPTURED BRAIN ARTERIOVENOUS MALFORMATIONS

2022

Brain arteriovenous malformations (bAVMs) are congenital defects of vasculogenesis, the natural history of which is characterized by a significant morbidity and mortality related to the risk of bleeding. Their management remains challenging, since complete eradication is often difficult. Embolization, surgery, or radiosurgery alone are safe and effective for small unruptured AVMs, while a multidisciplinary approach should be pursued for larger ones. We report a case of intracerebral haemorrhage due to the rupture of a large bAVM, for which a multidisciplinary approach was adopted: endovascular partial embolization followed by complete surgical removal.

Malformations of central nervous system: General issues

2013

Malformations of the central nervous system (CNS) encompass a heterogeneous group of congenital anomalies that may be isolated or appear as part of a genetic syndrome. Advances in identifying the genetic etiology underlying many CNS malformation and syndromes have led to the current genetic-based classifications that allows us to better estimate prognosis and potential complications. Herein, we discuss the main genetic, clinical and radiological features and their implications for diagnostic testing and disease management